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Hyperinsulinism: molecular aetiology of focal disease.
Ryan F, Devaney D, Joyce C, Nestorowicz A, Permutt MA, Glaser B, Barton DE, Thornton PS. Ryan F, et al. Among authors: permutt ma. Arch Dis Child. 1998 Nov;79(5):445-7. doi: 10.1136/adc.79.5.445. Arch Dis Child. 1998. PMID: 10193261 Free PMC article.
Genetic heterogeneity in familial hyperinsulinism.
Nestorowicz A, Glaser B, Wilson BA, Shyng SL, Nichols CG, Stanley CA, Thornton PS, Permutt MA. Nestorowicz A, et al. Among authors: permutt ma. Hum Mol Genet. 1998 Jul;7(7):1119-28. doi: 10.1093/hmg/7.7.1119. Hum Mol Genet. 1998. PMID: 9618169
Adenosine diphosphate as an intracellular regulator of insulin secretion.
Nichols CG, Shyng SL, Nestorowicz A, Glaser B, Clement JP 4th, Gonzalez G, Aguilar-Bryan L, Permutt MA, Bryan J. Nichols CG, et al. Among authors: permutt ma. Science. 1996 Jun 21;272(5269):1785-7. doi: 10.1126/science.272.5269.1785. Science. 1996. PMID: 8650576
Familial hyperinsulinism caused by an activating glucokinase mutation.
Glaser B, Kesavan P, Heyman M, Davis E, Cuesta A, Buchs A, Stanley CA, Thornton PS, Permutt MA, Matschinsky FM, Herold KC. Glaser B, et al. Among authors: permutt ma. N Engl J Med. 1998 Jan 22;338(4):226-30. doi: 10.1056/NEJM199801223380404. N Engl J Med. 1998. PMID: 9435328 Free article. No abstract available.
207 results